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Virologic and Immunologic Monitoring of Cytomegalovirus to Guide Preemptive Therapy in Solid-Organ Transplantation

机译:巨细胞病毒的病毒学和免疫学监测可指导实体器官移植中的抢先治疗

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Control of human cytomegalovirus (HCMV) infection during the posttransplant period was investigated in 134 solid-organ transplant recipients by monitoring in parallel virologic and immunologic parameters for at least 1 year of follow-up. Virologic monitoring was achieved by determining HCMV DNAemia with real-time PCR, using the threshold of 300 000 DNA copies/mL blood as a cutoff for starting preemptive therapy. Immunologic monitoring included measurement of HCMV-specific CD4+ and CD8+ T cells by cytokine flow cytometry, using HCMV-infected dendritic cells as a stimulus. HCMV infection was diagnosed in 110 (82%) and required treatment in 49 (36%) patients. At 12 months after transplantation ‘protective’ immunity (≥0.4 CD4+ and CD8+ HCMV-specific T cells/μL blood) was achieved in 115/129 (89%) patients. During the entire study period, 122 patients reconstituting HCMV-specific CD4+ and CD8+ T-cell immunity at 60 days posttransplant onward were able to control HCMV infection, except for one patient who developed HCMV disease because of a rejection episode. Patients reconstituting HCMV-specific CD8+ only did not control HCMV infection. In conclusion, the presence of both HCMV-specific CD4+ and CD8+ T cells ≥ 0.4/μL blood appears to be protective against HCMV disease. This result does not apply to patients undergoing antirejection treatment, or reconstituting HCMV-specific CD8+ T cells only.
机译:通过监测平行病毒学和免疫学参数至少1年的随访情况,对134名实体器官移植受者进行了移植后阶段人巨细胞病毒(HCMV)感染的控制研究。病毒学监测是通过实时PCR测定HCMV DNA的水平来实现的,使用300 000 DNA拷贝/ mL血的阈值作为开始抢先治疗的临界值。免疫学监测包括通过细胞因子流式细胞术,以感染HCMV的树突状细胞作为刺激,测量HCMV特异性CD4 +和CD8 + T细胞。 HCMV感染被诊断为110(82%),需要治疗的49(36%)患者。移植后12个月,在115/129(89%)患者中获得了“保护性”免疫(≥0.4 CD4 +和CD8 + HCMV特异性T细胞/μL血液)。在整个研究期间,有122名患者在移植后60天恢复了HCMV特异性CD4 +和CD8 + T细胞免疫,能够控制HCMV感染,但一名患者因排斥反应而发作了HCMV疾病。仅重组HCMV特异性CD8 +的患者不能控制HCMV感染。总之,血液中≥0.4 /μL的HCMV特异性CD4 +和CD8 + T细胞的存在似乎可以预防HCMV疾病。该结果不适用于接受抗排斥治疗或仅重建HCMV特异性CD8 + T细胞的患者。

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